Relative non-wettability of a purification membrane
Methods are herein provided for preparing a material for casting a flat-sheet, extruding a solid-fiber, and/or extruding a hollow-fiber utilizing a chlorinated aqueous amine solution as an effective solvent to form a crystalline polymorph structure of the material. This material in the form of, for example, an effective vapor permeable membrane can be used in membrane distillation to desalinate saline streams.
This application is a continuation-in-part of my allowed patent application Ser. No. 16/501,510 filed on Apr. 16, 2019; which is a continuation-in-part of my patent application Ser. No. 15/731,999 filed on Sep. 7, 2017, now U.S. Pat. No. 10,322,952; which is a continuation-in-part of my patent application Ser. No. 15/731,626 filed on Jul. 10, 2017, now U.S. Pat. No. 10,336,638; which is a continuation-in-part of my patent application Ser. No. 13/999,309 filed on Feb. 8, 2014, now U.S. Pat. No. 9,701,558.
This application is also related to my allowed patent application Ser. No. 16/501,595 filed on May 6, 2019; which is a continuation-in-part of my patent application Ser. No. 14/998,774 filed on Feb. 13, 2016, now U.S. Pat. No. 10,280,103; which is a continuation-in-part of my patent application Ser. No. 14/544,436 filed on Jan. 6, 2015, now U.S. Pat. No. 10,259,735; which is a continuation-in-part of my patent application Ser. No. 14/544,317 filed on Dec. 22, 2014, now U.S. Pat. No. 10,259,734; which is a continuation-in-part of my patent application Ser. No. 13/066,841 filed on Apr. 26, 2011, now U.S. Pat. No. 8,915,301.
BACKGROUND OF THE INVENTIONWater is the origin of every living thing. Yet the function of water—as a lubricant or a solvent, a displacing fluid or a displaced fluid, a wetting fluid or a non-wetted fluid, to name a few—firmly lies at the heart of physical situations that vary from geology (e.g., altering miscibility and interfacial forces), through biology (e.g., de-toxifying wastewater and derivative streams of wastewater), to oceanology (e.g., inverting the salinity of seawater to produce potable water and brine).
In saline water desalination, membrane distillation (MD) offers an elegant alternative concept to conventional methods [e.g., multi-stage flash (MSF) desalination, multi-effect (ME) distillation, and reverse osmosis (RO)], as energy efficient especially when combined with low grade or waste energy sources. MD has an essential simplicity of structure in that it consists inherently only of a compact housing envelop and a type of a low pressure separating surface performing only one function between two fluids at relatively moderate temperatures (e.g., <90° C.). However, vapor permeability through MD membranes is low; thereby enhancing it is of vital interest.
THE OBJECTIVES OF THE INVENTIONThe main objective of this invention is to provide membranes that can be extremely water non-wet and extremely permeable to wetting fluids including vapor.
BRIEF SUMMARY OF THE INVENTIONThe present invention generally provides methods for preparing a material for casting a flat-sheet, extruding a solid-fiber, and/or extruding a hollow-fiber utilizing a chlorinated aqueous amine solution as an effective solvent for phase inverting the material to form a crystalline polymorph structure.
The inventive materials are not restricted to use in connection with one particular application. They can be used, in general, to separate water vapor from saline water in MD, to separate gases and hydrophobic constituents from wastewater, to separate gases and/or oil from wet oil. Further objects, novel features, and advantages of the subject invention will be apparent to those skilled in the art upon examining the accompanying drawings and upon reading the following description of the preferred embodiments, or may be learned by practice of the invention. Those of ordinary skills in the art will appreciate that the subject invention can be modified or adapted in a variety of ways. All such modifications or adaptions, which fall within the scope of the appended claims, are intended to be covered.
Phase inversion has been appeared in a multitude of forms, but all have been characterized by specific controls of composition (e.g., solubility, pH, etc.), temperature, pressure, and/or combinations thereof. Phase inversion is also used as an enabling step in the work-up or break-up of a reaction or an interaction, before final displacement of a phase, before final casting or extruding of a phase, or before final separation/purification of a phase or a product by distillation, filtration, sublimation, precipitation, crystallization, adsorption, absorption, among others.
Precipitation, for example, involves phase inversion, wherein a soluble species in a primary solvent is transformed into an insoluble state either by decreasing its solubility in the primary solvent or by extracting the primary solvent from the soluble species. One form is selective precipitation, which stands on inducing a secondary solvent to a solution to reduce the solubility of the species by binding the primary solvent to the secondary solvent. Of course, the identity of the primary solvent, the nature and concentration of the soluble species and the conditions under which phase inversion is conducted come into play, but the effectiveness resides with the identity and modification of the secondary solvent.
The induction of an amine solvent [e.g., methylamine (ME), ethylamine (EA), isopropylamine (IPA), propylamine (PA), dimethylamine (DMA), diethylamine (DEA), diisopropylamine (DTA) and dipropylamine (DPA)] has been innovatively used by the inventor as a secondary solvent in a liquid phase precipitation as well as a vapor (compressed and/or flashed) phase precipitation with multiple variants to effectively selectively precipitate targeted: (1) inorganic species; and/or (2) ionizable organics (e.g., carboxylic salts, phenol salts, etc.) and inorganics (e.g., carbonates, sulfides, etc.) from aqueous streams. The yields of these precipitation variants are remarkable particularly, for example, in: (1) de-scaling saline streams; (2) aiding the de-oiling of saline streams; (3) de-mixing the amphiphilic portion of wet oil; and (4) de-folding the amphiphilic nature of proteins in wastewater to ultimately separate endotoxins with dense gas (e.g., carbon dioxide).
The key factors in these selective precipitation variants are that the amine solvent (the secondary solvent) is miscible with water (the primary solvent), whereas: (1) the solubility of the targeted inorganic species is very limited in the amine solvent; and/or (2) the ionizablity of targeted organic and inorganic species in the presence of the amine solvent becomes crossover (below or above) the neutral pH. The latter has been further modified by, for example, transforming the amine solvent into an anionated form by reacting it with acid, since these amine solvents are weak bases that undergo reversible reactions with water or acid to form weak acids, and then regenerating the amine solvent (a weak base) from its anionated form by an external hydroxide source (an inorganic or organic). The external hydroxide source serves, in turn, a multitude of purposes including restoring the amine solvent to its weak basic form to serve a further purpose, facilitating the recovery of the amine solvent for reuse, and using the external hydroxide source, itself, in a further step (e.g., de-scaling). This pH switchability of the amine solvent displaces selectively the ionization equilibrium of reactive species towards either their molecular forms or ionized states. It displaces the ionization equilibrium of, for example, carboxylic acids and phenols in wet oil towards their molecular forms under an acidic condition, which are essentially hydrophobic instead of their amphiphilic ionized states under slightly basic conditions. The opposite goes for naturally occurring basic constituents in wet oil. The pH switchability thus leads to two low values of wet oil interfacial tension; one at either end of the pH scale.
As such, the inventor has innovatively exploited the competition between targeted inorganic species and/or ionizable species and amine molecules on the water molecules by: (1) the “amining out” step wherein targeted inorganic species are precipitated whereas the amine solvent remains in solution; (2) “salting out” step wherein an amine solvent is separated while inorganic species remains in the solution; (3) the “ionizing out” step wherein acidic and basic ionizable organic and inorganic species and proteins are reversibly selectively displaced by dissolving them, precipitating them, isolating them, and/or converting them to a gaseous state whereas the amine solvent remains in solution; (4) the “wetting out” step wherein a membrane's pores are selectively filled with a liquid phase or fluid; and/or (5) the standalone, sequential or simultaneous occurrence of such described steps. The fundamental thermodynamic frameworks for the precipitation of ionic species in mixed solvents have also been established [Bader; 1998 and 1999].
Phase inversion by inducing a secondary solvent has also long been used, among other concepts (e.g., melting, sintering, etching, stretching, surface coating, surface grafting, etc.), to prepare membranes. In a conventional polymer phase inversion process comprising three components, a polymer is dissolved in a primary solvent to form a homogenous solution. The polymer is then precipitated from the homogenous solution by a secondary solvent, wherein the secondary solvent is soluble in the primary solvent while the polymer is nearly insoluble in the secondary solvent. During phase de-mixing, the solution is cast (e.g., flat-sheet) or extruded (e.g., hollow-fiber, tubular, etc.) into a desired shape, wherein the polymer-rich phase solidifies into a membrane matrix whereas the polymer-poor phase develops into pores within the membrane. The thermodynamic principle for the precipitation of polymeric species in mixed solvents has been delineated [e.g., Hsu and Prausnitz, 1974]. In different variants of inducing a secondary solvent, polymer phase inversion by precipitation has been used to prepare membranes. The basic principles of these variants are briefly summarized in the following paragraph [e.g., Ferry, 1936].
A membrane film was historically practically prepared by subjecting a polymer dissolved in a primary solvent to vapor of a secondary solvent to prevent the evaporation of the primary solvent from the formed film but allow the vapor of the secondary solvent to diffuse into the formed film, thereby forming a porous membrane without a top layer. Here, the secondary solvent is more volatile than the primary solvent. In another variant, a polymer is dissolved in mixed primary and secondary solvents, wherein the primary solvent is more volatile than the secondary solvent, whereby increasing the content of the polymer and secondary solvent by evaporating the primary solvent, which eventually leads to polymer precipitation resulting in forming a skinned membrane. In a further variant, a polymer is dissolved in a primary solvent, and the homogenous solution is cast on a substrate by dip coating or spraying, followed by allowing the primary solvent to evaporate in an inert atmosphere (e.g., nitrogen or air) to expel the vapor of the primary solvent, thereby forming a dense homogenous membrane. Phase inversion by these evaporative precipitation variants has been further adapted to prepare membranes by liquid-phase precipitation, wherein a homogenous solution comprising a polymer and a primary solvent is directly immersed in a bath containing a secondary solvent [e.g., Loeb and Sourirajan, 1963]. The latter made the practical use of reverse osmosis (RO) hydrophilic membranes to desalinate seawater possible, which was a landmark contribution of United States to the desalination field. Membrane fabrications since then remain essentially extensions of such methods; all which involve melting or dissolving a polymer, casting or extruding the melted or dissolved polymer, and precipitating the polymer by phase inversion; but again the effectiveness resides with the identity and modification of the secondary solvent.
Precedent surface modification methods for polytetrafluoroethylene (PTFE) to make it bondable to other materials by reacting the surface with suitable fluid cation/metal reactants before bonding were developed in the 1950s [U.S. Pat. No. 2,789,063]. The methods were based on replacing fluorine in the surface layer of PTFE with the cation or metal, thereby making the surface more hydrophilic. Alkali cations (e.g., sodium), alkaline earth cations (e.g., calcium), and transition metals (e.g., manganese or zinc) were used to react with PTFE surfaces at high temperatures [e.g., above the melting point of the cation or metal, but below the melting point of PTFE (315° C.)] or heating the PTFE material as it emerged from a liquid reacting bath at high temperatures (e.g., 220° C.); wherein the cation or metal is a vapor, a cation or metal hydride, or in non-aqueous liquid ammonia or methylamine. It should also be noted that, as all hydroflurocarbon polymers, pyrolysis at high temperatures also degrades PVDF by the evolution of a large amount of hydrogen fluoride (HF). This large loss of HF, de-hydrofluorination, is due to the equal distribution of repeated hydrogen-fluoride chains in PVDF. De-hydrofluorination may be followed by the formation of double bonds (chain scission, thereby more thermal stability), and/or may result in cross-linking of the polymer (fusing, thereby highly orientated fibrils and better mechanical strength). The de-hydrofluorination mechanisms of PVDF by pyrolysis may be expressed as follows [Madorsky, 1964].
Chemically, rather than thermally, cross-linking modifications of PVDF and/or equivalent materials to produce highly orientated interlinked semi-crystalline particle or globular structures is the underpinning objective of this invention. This can be achieved without replacing fluorine from the surface layer of a hydroflurocarbon polymer at high temperatures or degrading the bulk of the hydroflurocarbon polymer by pyrolysis. Thus, this invention provides methods for obtaining desired surface effects of PVDF or equivalent materials, which will now be explained by several points and illustrated by various non-limitative embodiments.
First, PVDF possesses two valuable properties of practical importance, which are the polymorphic and piezoelectric properties. In regards to the polymorphic properties, PVDF is a border line hydrophobic (Table 1) semi-crystalline polymer that is approximately 50% amorphous; wherein the monomer's structure is [—CH2—CF2—], and the repeated chains occur mostly in a head to tail configuration. PVDF can be dissolved at low temperatures (e.g., <60° C.) in an organic solvent (as a primary solvent) such as N,N-dimethylacetamide (DMA), N,N-dimethylformamide (DMF), dimethylsulfoxide (DMSO), hexamethyl phosphoramide (HMPA), N-methyl-2-pyrrolidone (NMP), tetramethylurea (TMU), triethyl phosphate (TEP), trimethyl phosphate (TMP), acetone, methyl ethyl ketone (MEK), tetrahydrofuran (THF), and/or combinations thereof. This is unlike some hydroflurocarbon polymers such as PTFE (Teflon) or other hydrophobic plastic materials such as polyethylene (PE) and polypropylene (PP). Because of its solubility in such solvents, the fabrication of PVDF membranes via wet, rather than melt, phase inversion methods is possible. Since PVDF is insoluble in water, the repeatedly reported medium (e.g., as a secondary solvent) for fabricating PVDF via phase inversion is usually water with or without peroxy compounds (e.g., containing the divalent group O—O) acting as polymerization catalysts. In regards to the piezoelectric properties (e.g., transfer mechanical energy to electrical energy and vice versa), the high Curie point (103° C.; the temperature above which the piezoelectric effect breaks down), and the response to an electric potential by acting along the backbone make PVDF a valuable material. Other useful properties of PVDF include high elastic modulus and high rigidity (resists deformation); resistance to heat, combustion, ageing and abrasion; chemically inert and non toxic; and stability to radiation (X-ray, UV and Gamma).
Second, one of the utilities of the polymorphic properties of PVDF is to form membranes. Recalling that a raw polymer must be soluble in a primary solvent, and, in turn, the primary solvent must be soluble in a secondary solvent, whereas the polymer is insoluble in the secondary phase; thereby de-mixing the polymer, as it is forced out of the primary solvent by the secondary solvent, into a polymer-rich phase and a surrounding polymer-lean solution. However, the polymer-rich phase may be dominated by amorphous particles (precipitation), pure crystalline polymorph particles (crystallization), or a concurrent combination of precipitation and crystallization. The differences among them lie in the formation process and the final product formed. As is the nature of this type of phase inversion, the formation process (the thereby predominance of either one) requires a proper effective secondary solvent and a precise control over the conditions (e.g., the rate of induction-time as related to instant or delayed de-mixing, and the rate of mass transfer as related to the level of saturation and stability) under which the thermodynamic and kinetic phase behaviors of the forming membrane are dictated. In this invention, crystallization of PVDF or an equivalent material is sought out to form effective and inexpensive membranes.
Third, amine solvents [including methylamine (ME), ethylamine (EA), isopropylamine (IPA), propylamine (PA), dimethylamine (DMA), diethylamine (DEA), diisopropylamine (DIPA), dipropylamine (DPA), trimethylamine (TMA), triethylamine (TEA), tripropylamine (TPA)] are unexpectedly found to be effective in crystallizing PVDF or an equivalent material to form the sought out membranes and other articles. Such amine solvents are weak bases, which do not generate hydroxyl ions directly by dissociation, but by reaction with water. For example, IPA reacts with water as follows:
CH3CH2CH2NH2+H2O⇔CH3CH2CH2NH3+OH− (2)
Yet, most weak bases are anions. For example, the fluoride ion is a weak base anion, which undergoes a similar reversible reaction with water as follows:
F−+H2O⇔HF+OH− (3)
In both cases of such weak bases, the forward reactions occur only to a slight extent to produce a weak acid (e.g., CH3CH2CH2NH3+; HF); and an enough OH− ion to make the solution basic. Further, the reaction of the amine solvent (IPA for example) with hydrofluoric acid generates the amine solvent in an anionated form as follows:
CH3CH2CH2NH2+HF→CH3CH2CH2NH3+F (4)
Here, the novelty of this invention resides with the use of an aqueous amine solvent as a weak base, thereby not as a strong denature, to pre-treat a solution of PVDF (or an equivalent material) dissolved in a primary solvent before phase inverting the solution; wherein the aqueous amine solvent gently draws some of the inorganic fluorine from the water-insoluble PVDF polymer for reaction, thereby generating the hydrofluoric acid by de-hydrofluorinating the PVDF; wherein implicit in this pre-treatment is the further reaction of the generated hydrofluoric acid with the aqueous amine solvent to regenerate the amine solvent in the anionated (fluorine) form; and wherein the amine solvent in the anionated form, as a weak anion base, represents a further step that draws in an essentially similar manner some of the fluorine from the water-insoluble PVDF polymer; thereby OH− ions are dissociated from the aqueous amine solvent, the released fluorine anion from PVDF and the amine solvent in the anionated form to diffuse in the PVDF polymer and bring it to reaction. The combined effects of the aqueous amine solvent and the amine solvent in the anionated form, which are not strong denaturants, minimize the disruption of inter-molecular interactions in PVDF (or an equivalent material), and leads to the formation of very fine crystalline clusters. The implication of this novelty of molecular interactions is that they serve as gentle re-crystallization media prior to phase inverting the PVDF solution.
Fourth, Table 2 presents the liquid surface tensions of water and the amine solvents. The liquid surface tensions (σL) of such amine solvents are not only much lower than σL of water (Table 2), but also lower than the critical surface tension (σC) of PVDF (Table 1). Here, σC is the surface tension at which a liquid just completely wets a surface (θ=0). The ability of such an aqueous amine solvent to spread through the low energy PVDF solution depends on the volume fraction of the amine solvent in water to depress the surface tension of water (σL) in the aqueous amine solution (σS) preferably below σC of PVDF. For example, σL of C3H9N [Table 2; (TMA: 13.4 mN/m; IPA: 17.5 mN/m)] is roughly about half σC of PVDF [Table 1; (31.6 mN/m)].
where xi is the mole fraction and vi is the pure solvent molar volume. A relatively small volume fraction of most of such amine solvents would thus reduce the interfacial tension of the aqueous amine solution to about or below σC of PVDF. It follows from the definition of σC and the insolubility of PVDF in pure water that the novelty of this invention further resides in sufficiently lowering the surface tension of water in the aqueous amine solution by the amine solvent; thereby largely delaying the instantaneous de-mixing (precipitation) power of pure water prior to phase inverting the PVDF solution.
Fifth, the pores in a hydrophobic membrane are filled with the fluid that wets the membrane. The non-wetting fluid (water) does not permeate into pores of the membrane as long as the pressure on the non-wetting fluid side is kept below a critical value, which is known as the “liquid entry” or “breakthrough” pressure. For gas-liquid contacting (e.g., vapor-water as in MD) or liquid-liquid extraction (e.g., de-mixing oil and water phases from wet-oil), the “liquid entry” pressure of water (the non-wetting fluid) may be roughly approximated as follows:
where σ may refer to as the surface tension in the case of vapor-liquid contacting or the interfacial tension in the case of liquid-liquid contacting, θw is the water contact angle of the membrane, and r is the pore radius of the membrane. Eq. (6) implies that the higher the water contact angle and the lower pore radius of the membrane, the higher is the liquid entry pressure of water. It follows from the definition of ΔPE and the insolubility of PVDF in pure water that the novelty of this invention yet further resides in substantially increasing the water contact angle of the membrane by the aqueous amine solution and substantially decreasing the pore size of the membrane by limiting the water content in the aqueous amine solution prior to phase inverting the PVDF solution.
The hydroflurocarbon polymer [P] is selected from the group consisting of polyvinylidene fluoride (PVDF), polytrifluoroethylene (PFE), polychlorotrifluoroethylene (PCFE), fluorinated ethylene propylene (FEP), polyhexafluoropropylene (PHFP), and/or combinations thereof.
The primary solvent to dissolve the polymer is selected from the group consisting of N-methyl-2-pyrrolidone (NMP), N,N-dimethylacetamide (DMA), N,N-dimethylformamide (DMF), dimethylsulfoxide (DMSO), hexamethyl phosphoramide (HMPA), tetramethylurea (TMU), triethyl phosphate (TEP), trimethyl phosphate (TMP), acetone, methyl ethyl ketone (MEK), tetrahydrofuran (THF), and/or combinations thereof.
The amine solvent to form the aqueous amine solution is selected from the group consisting of methylamine (ME), ethylamine (EA), isopropylamine (IPA), propylamine (PA), dimethylamine (DMA), diethylamine (DEA), diisopropylamine (DTPA), dipropylamine (DPA), trimethylamine (TMA), triethylamine (TEA), tripropylamine (TPA), and/or combinations thereof.
Thus, successful flat-sheet membranes were made according to this invention in a multitude of variants. For example, in one variant, a PVDF powder (as a polymer [P]) and NMP (as a primary solvent [1A]) were mixed to form a homogenous first solution [FS] (3 vol % [P]: 97 vol % [1A]). IPA [2A] and water [3A] were mixed to form an aqueous amine solution [AAS]; wherein φ of IPA in water was about 0.23 (about 6 mol %), which corresponded to about 31.1 mN/m of σL the aqueous amine solution. Different amounts [10] of the aqueous amine solution [AAS] were then mixed with fixed amounts [FS1] of the first solution [FS] to form several second solutions [SS]. Each of the second solutions was casted on an inert substrate, each of the casted substrate was immersed in a bath containing only water for phase inversion, and each of the formed flat-sheet membranes is removed from each substrate and washed with water.
When chlorine is introduced into water; as chlorine gas (Cl2), hypochlorite (ClO−) in the form of sodium or calcium, or in other forms, it rapidly undergoes hydrolysis to produce mainly hypochlorous acid (HClO); wherein the latter is a weak acid that dissociates in aqueous solution as follows:
HClO+H2O⇔ClO−+H++H2O (7)
If an amine solvent (IPA for example) is reacted with hypochlorous acid, it will generate the amine solvent in a monochloroamine form as follows:
CH3CH2CH2NH2+HClO→CH3CH2CH2NHCl+H2O (8)
If the source of chlorine is chlorine gas, the hydrolysis of the chlorine gas will also produce hydrochloric acid in addition to the dominant hypochlorous acid. The amine solvent (IPA for example) also reacts with hydrochloric acid to regenerate the amine solvent in an anionated form as follows:
CH3CH2CH2NH2+HCl→CH3CH2CH2NH3+Cl (9)
In addition to utility of an aqueous amine solution as described in Paragraphs [0029] and [0030], the novelty of this invention further resides with the use of a chlorinated aqueous amine solvent (e.g., CH3CH2CH2NHCl) to serve as a pore enlarger; thereby enhancing the vapor permeability of PVDF or an equivalent material.
The chlorine source is selected from the group consisting of chlorine gas, hypochlorite, and/or combinations thereof.
A flat-sheet configuration is very useful in different applications including, for example, replacing conventional coalescing packings of a 3-phase separator in an oil gathering center by the invented flat-sheets in submerged membrane modules to effectively directly simultaneously separate gas and oil from water within the 3-phase separator, wastewater membrane bioreactors, among other applications. A solid-fiber configuration utilizing the piezoelectric property of PVDF is very useful in different applications including, for example, energy harvesters (e.g., solar panels), mechanical actuators, strain sensors, artificial muscles, and nearly completely non-porous membranes for higher pressure applications. A hollow-fiber configuration is also very useful in, for example, a gas-liquid or a liquid-liquid contactor especially for standalone membrane applications. However, the three essential formation differences among these configurations are morphology, viscosity, and tension/stress. For a flat-sheet configuration or a solid-fiber configuration, morphology adjustments start naturally from the outer surface of a cast or extrude film after immersing in a phase inverting bath. For a hollow-fiber configuration, morphology adjustments are simultaneously required for the inner (lumen side) and the outer (shell side) surfaces, wherein the inner surface is controlled by a bore fluid (e.g., liquid or gas) as an internally phase inverting media, and wherein the outer surface is controlled by a solvent in an externally phase inverting bath. The required viscosity for a polymer solution (a dissolved polymer in a primary solvent) for spinning a solid-fiber or a hollow-fiber may be an order of magnitude higher than that for casting a flat-sheet; thereby the required amount of the polymer for the solid-fiber or the hollow-fiber may be in the order of 3-times the required amount for the flat-sheet. Unlike the formation of the flat-sheet, the solid-fiber or the hollow-fiber is usually formed under tension and/or stress.
The above described inventive methods of utilizing an aqueous amine solution or a chlorinated aqueous amine solution are aimed at semi-crystalline polymers; wherein fine crystal clusters are selectively and relatively slowly formed from a polymer dissolved in a primary solvent by such amine solutions resulting in crystalline polymorph structures. Generated hydrophilic membranes by phase inverting glassy polymers (e.g., polysulfone, cellulose acetate, regenerated cellulose, nitrocellulose, polyamide, polyimide, etc.) usually involved very rapid precipitation resulting in amorphous macro-void structures. However, the utilization of an aqueous amine solution or a chlorinated aqueous amine solution as described in this invention can be extended to such glassy polymers to form membranes with the structures free of such undesirable macro-voids.
Claims
1. A method of preparing a purification membrane by casting a flat-sheet, said method comprising the steps of: (a) dissolving an amount of a polymer in an amount of a primary solvent to form a first solution; (b) mixing an amount of an amine solvent, an amount of water, and an amount of a chlorine source to form a chlorinated aqueous amine solution; (c) mixing an amount of said first solution with an amount of said chlorinated aqueous amine solution to form a second solution; thereby inducing selective fine crystal clusters of said polymer, without rapidly precipitating said polymer, and without degrading the bulk of the structure of said polymer; (d) casting an amount of said second solution on a substrate; and (e) phase inverting said substrate in a bath containing only water to form said flat-sheet.
2. The method of claim 1, wherein said polymer is selected from the group consisting of polyvinylidene fluoride, polytrifluoroethylene, polychlorotrifluoroethylene, fluorinated ethylene propylene, polyhexafluoropropylene, and combinations thereof.
3. The method of claim 1, wherein said primary solvent is selected from the group consisting of N-methyl-2-pyrrolidone, N,N-dimethylacetamide, N,N-dimethylformamide, dimethylsulfoxide, hexamethyl phosphoramide, tetramethylurea, triethyl phosphate, trimethyl phosphate, acetone, methyl ethyl ketone, tetrahydrofuran, and combinations thereof.
4. The method of claim 1, wherein said amine solvent is selected from the group consisting of methylamine, ethylamine, isopropylamine, propylamine, dimethylamine, diethylamine, diisopropylamine, dipropylamine, trimethylamine, triethylamine, tripropylamine, and combinations thereof.
5. The method of claim 1, wherein said chlorine source is selected from the group consisting of chlorine gas, hypochlorite, and combinations thereof.
6. A method of preparing a purification membrane by extruding a solid-sheet, said method comprising the steps of: (a) dissolving an amount of a polymer in an amount of a primary solvent to form a first solution; (b) mixing an amount of an amine solvent, an amount of water, and an amount of a chlorine source to form a chlorinated aqueous amine solution; (c) mixing an amount of said first solution with an amount of said chlorinated aqueous amine solution to form a second solution; thereby inducing selective fine crystal clusters of said polymer, without rapidly precipitating said polymer, and without degrading the bulk of the structure of said polymer; (d) extruding an amount of said second solution through a spinneret to produce an extruded solid fiber; and (e) phase inverting said extruded solid fiber in at least a bath containing only water to form said solid-sheet.
7. The method of claim 6, further comprising replacing the steps (c) through (e) by the following steps: extruding an amount of said first solution through said spinneret to produce said extruded fiber; subjecting said extruded fiber to a bath containing an amount of said chlorinated aqueous amine solution; and thereafter phase inverting said extruded solid fiber in said bath containing said only water to form said solid-sheet.
8. The method of claim 6, wherein said polymer is selected from the group consisting of polyvinylidene fluoride, polytrifluoroethylene, polychlorotrifluoroethylene, fluorinated ethylene propylene, polyhexafluoropropylene, and combinations thereof.
9. The method of claim 6, wherein said primary solvent is selected from the group consisting of N-methyl-2-pyrrolidone, N,N-dimethylacetamide, N,N-dimethylformamide, dimethylsulfoxide, hexamethyl phosphoramide, tetramethylurea, triethyl phosphate, trimethyl phosphate, acetone, methyl ethyl ketone, tetrahydrofuran, and combinations thereof.
10. The method of claim 6, wherein said amine solvent is selected from the group consisting of methylamine, ethylamine, isopropylamine, propylamine, dimethylamine, diethylamine, diisopropylamine, dipropylamine, trimethylamine, triethylamine, tripropylamine, and combinations thereof.
11. The method of claim 6, wherein said chlorine source is selected from the group consisting of chlorine gas, hypochlorite, and combinations thereof.
12. A method of preparing a purification membrane by extruding a hollow fiber, said method comprising the steps of: (a) dissolving an amount of a polymer in a first amount of a primary solvent to form a first solution; (b) mixing an amount of an amine solvent, an amount of water, and an amount of a chlorine source to form a chlorinated aqueous amine solution; (c) mixing an amount of said first solution with a first amount of said chlorinated aqueous amine solution to form a second solution; thereby controlling the morphology of the outer surface of said hollow fiber; (d) mixing a second amount of said primary solvent with a second amount of said chlorinated aqueous amine solution to form a bore liquid; thereby controlling the morphology of the inner surface of said hollow fiber; (e) extruding an amount of said second solution and an amount of said bore liquid through a spinneret to produce an extruded hollow-fiber; and (f) phase inverting said extruded hollow-fiber in at least a bath containing only water to form said hallow-fiber.
13. The method of claim 12, further comprising replacing step (d) by: mixing said second amount of said primary solvent with an amount of water to form said bore liquid.
14. The method of claim 12, further comprising replacing steps (c), (e) and (f) by the following steps: extruding an amount of said first solution and an amount of said bore liquid through said spinneret to produce said extruded hollow-fiber; subjecting said extruded hollow-fiber to a bath containing an amount of said chlorinated aqueous amine solution; and thereafter phase inverting said extruded hollow-fiber in said bath containing only water to form said hollow-fiber.
15. The method of claim 12, further comprising replacing steps (c) through (f) by the following steps: mixing said second amount of said primary solvent with an amount of water to form said bore liquid; extruding an amount of said first solution and an amount of said bore liquid through said spinneret to produce said extruded hollow-fiber; subjecting said extruded hollow-fiber to a bath containing an amount of said chlorinated aqueous amine solution; and thereafter phase inverting said extruded hollow-fiber in said bath containing only water to form said hollow-fiber.
16. The method of claim 12, wherein said polymer is selected from the group consisting of polyvinylidene fluoride, polytrifluoroethylene, polychlorotrifluoroethylene, fluorinated ethylene propylene, polyhexafluoropropylene, and combinations thereof.
17. The method of claim 12, wherein said primary solvent is selected from the group consisting of N-methyl-2-pyrrolidone, N,N-dimethylacetamide, N,N-dimethylformamide, dimethylsulfoxide, hexamethyl phosphoramide, tetramethylurea, triethyl phosphate, trimethyl phosphate, acetone, methyl ethyl ketone, tetrahydrofuran, and combinations thereof.
18. The method of claim 12, wherein said amine solvent is selected from the group consisting of methylamine, ethylamine, isopropylamine, propylamine, dimethylamine, diethylamine, diisopropylamine, dipropylamine, trimethylamine, triethylamine, tripropylamine, and combinations thereof.
19. The method of claim 12, wherein said chlorine source is selected from the group consisting of chlorine gas, hypochlorite, and combinations thereof.
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Type: Grant
Filed: Feb 8, 2020
Date of Patent: Mar 2, 2021
Inventor: Mansour S. Bader (College Station, TX)
Primary Examiner: Nina Bhat
Application Number: 16/873,135
International Classification: B01D 15/00 (20060101); C02F 9/00 (20060101); C02F 1/00 (20060101); C02F 1/20 (20060101); C02F 1/52 (20060101); C02F 1/54 (20060101); C02F 1/44 (20060101); C02F 1/72 (20060101); C02F 103/18 (20060101);
